Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700129C05Rik |
T |
C |
14: 59,377,079 (GRCm39) |
N105D |
possibly damaging |
Het |
A2m |
T |
C |
6: 121,615,231 (GRCm39) |
|
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,415,198 (GRCm39) |
N641S |
probably damaging |
Het |
Aff4 |
T |
A |
11: 53,263,708 (GRCm39) |
S243T |
probably benign |
Het |
Agap2 |
A |
G |
10: 126,923,764 (GRCm39) |
H713R |
unknown |
Het |
Ap2a2 |
T |
A |
7: 141,211,206 (GRCm39) |
M914K |
probably damaging |
Het |
Bcl7c |
A |
T |
7: 127,307,635 (GRCm39) |
M22K |
possibly damaging |
Het |
Cacna1i |
A |
T |
15: 80,256,663 (GRCm39) |
D1019V |
probably damaging |
Het |
Cd7 |
T |
C |
11: 120,929,012 (GRCm39) |
T80A |
probably benign |
Het |
Chia1 |
T |
C |
3: 106,029,755 (GRCm39) |
Y130H |
probably damaging |
Het |
Chmp6 |
T |
C |
11: 119,808,872 (GRCm39) |
|
probably benign |
Het |
Chrnb4 |
A |
G |
9: 54,942,878 (GRCm39) |
V132A |
probably benign |
Het |
Ctnna3 |
A |
G |
10: 63,402,619 (GRCm39) |
D110G |
probably benign |
Het |
Cyp2d37-ps |
A |
T |
15: 82,573,975 (GRCm39) |
|
noncoding transcript |
Het |
Dnah6 |
T |
C |
6: 72,998,240 (GRCm39) |
M4061V |
probably benign |
Het |
Dydc2 |
C |
A |
14: 40,783,903 (GRCm39) |
M73I |
probably benign |
Het |
Egflam |
G |
T |
15: 7,319,475 (GRCm39) |
|
probably null |
Het |
Fam228b |
C |
T |
12: 4,798,351 (GRCm39) |
V151I |
possibly damaging |
Het |
Fanca |
C |
T |
8: 124,031,552 (GRCm39) |
V380I |
probably damaging |
Het |
Gbp2b |
T |
C |
3: 142,313,944 (GRCm39) |
L408S |
probably damaging |
Het |
Kcnh4 |
T |
C |
11: 100,648,507 (GRCm39) |
S66G |
probably benign |
Het |
Kcnq3 |
A |
T |
15: 65,892,154 (GRCm39) |
V407D |
possibly damaging |
Het |
Kif24 |
A |
T |
4: 41,428,413 (GRCm39) |
D182E |
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,740,818 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
T |
A |
14: 102,114,313 (GRCm39) |
N140K |
probably damaging |
Het |
Myo5c |
A |
G |
9: 75,204,701 (GRCm39) |
E1518G |
probably damaging |
Het |
Myof |
A |
T |
19: 38,012,793 (GRCm39) |
N47K |
probably damaging |
Het |
Nckap1 |
G |
T |
2: 80,375,321 (GRCm39) |
|
probably benign |
Het |
Nlrp1a |
C |
A |
11: 71,014,501 (GRCm39) |
G250W |
probably damaging |
Het |
Nol4l |
T |
A |
2: 153,253,672 (GRCm39) |
S390C |
probably benign |
Het |
Or2ag2b |
T |
C |
7: 106,417,908 (GRCm39) |
F206S |
probably benign |
Het |
Or52e18 |
T |
A |
7: 104,609,388 (GRCm39) |
M184L |
probably damaging |
Het |
Or5ak22 |
T |
C |
2: 85,230,685 (GRCm39) |
Q64R |
possibly damaging |
Het |
Or5h26 |
G |
A |
16: 58,988,269 (GRCm39) |
P79L |
possibly damaging |
Het |
Plec |
G |
T |
15: 76,061,367 (GRCm39) |
P2886T |
probably damaging |
Het |
Prdm16 |
T |
C |
4: 154,425,568 (GRCm39) |
Y738C |
probably benign |
Het |
Ptprz1 |
A |
G |
6: 23,016,164 (GRCm39) |
Y820C |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Sgce |
G |
A |
6: 4,718,019 (GRCm39) |
P98S |
probably damaging |
Het |
Siglecf |
T |
C |
7: 43,001,368 (GRCm39) |
F112S |
probably damaging |
Het |
Slc6a16 |
C |
T |
7: 44,908,672 (GRCm39) |
A84V |
possibly damaging |
Het |
Sntb2 |
T |
C |
8: 107,728,170 (GRCm39) |
S373P |
probably damaging |
Het |
Sorcs2 |
C |
T |
5: 36,185,218 (GRCm39) |
V953I |
probably benign |
Het |
Spata31f1a |
T |
C |
4: 42,851,116 (GRCm39) |
I347V |
probably benign |
Het |
St7l |
T |
C |
3: 104,803,125 (GRCm39) |
|
probably benign |
Het |
Stap2 |
A |
G |
17: 56,307,097 (GRCm39) |
V217A |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,108,670 (GRCm39) |
D215E |
probably damaging |
Het |
Synm |
C |
T |
7: 67,385,569 (GRCm39) |
V256I |
probably benign |
Het |
Syt13 |
A |
C |
2: 92,776,412 (GRCm39) |
E233A |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,295,514 (GRCm39) |
E327V |
probably damaging |
Het |
Tent5b |
A |
T |
4: 133,213,522 (GRCm39) |
Q131L |
probably benign |
Het |
Themis3 |
A |
T |
17: 66,866,540 (GRCm39) |
|
probably null |
Het |
Ttll13 |
T |
A |
7: 79,897,084 (GRCm39) |
D14E |
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,734,584 (GRCm39) |
|
probably null |
Het |
Vps13d |
A |
T |
4: 144,844,195 (GRCm39) |
V2537E |
possibly damaging |
Het |
Zscan10 |
T |
A |
17: 23,829,056 (GRCm39) |
F456I |
probably damaging |
Het |
Zyg11b |
A |
G |
4: 108,123,604 (GRCm39) |
I121T |
probably damaging |
Het |
|
Other mutations in Tubb2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01683:Tubb2a
|
APN |
13 |
34,260,530 (GRCm39) |
critical splice donor site |
probably null |
|
R0233:Tubb2a
|
UTSW |
13 |
34,259,325 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0233:Tubb2a
|
UTSW |
13 |
34,259,325 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2033:Tubb2a
|
UTSW |
13 |
34,259,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Tubb2a
|
UTSW |
13 |
34,259,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R3836:Tubb2a
|
UTSW |
13 |
34,259,294 (GRCm39) |
missense |
probably benign |
0.30 |
R3837:Tubb2a
|
UTSW |
13 |
34,259,294 (GRCm39) |
missense |
probably benign |
0.30 |
R3839:Tubb2a
|
UTSW |
13 |
34,259,294 (GRCm39) |
missense |
probably benign |
0.30 |
R4879:Tubb2a
|
UTSW |
13 |
34,258,572 (GRCm39) |
missense |
probably benign |
0.02 |
R4936:Tubb2a
|
UTSW |
13 |
34,259,240 (GRCm39) |
nonsense |
probably null |
|
R5537:Tubb2a
|
UTSW |
13 |
34,259,434 (GRCm39) |
missense |
probably benign |
0.07 |
R5889:Tubb2a
|
UTSW |
13 |
34,259,451 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6102:Tubb2a
|
UTSW |
13 |
34,259,326 (GRCm39) |
missense |
probably benign |
0.00 |
R6475:Tubb2a
|
UTSW |
13 |
34,259,442 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7206:Tubb2a
|
UTSW |
13 |
34,259,505 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7254:Tubb2a
|
UTSW |
13 |
34,258,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Tubb2a
|
UTSW |
13 |
34,259,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:Tubb2a
|
UTSW |
13 |
34,259,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R7734:Tubb2a
|
UTSW |
13 |
34,258,776 (GRCm39) |
missense |
probably benign |
0.06 |
R7815:Tubb2a
|
UTSW |
13 |
34,258,962 (GRCm39) |
missense |
probably benign |
0.10 |
R7850:Tubb2a
|
UTSW |
13 |
34,258,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:Tubb2a
|
UTSW |
13 |
34,258,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R9170:Tubb2a
|
UTSW |
13 |
34,260,628 (GRCm39) |
missense |
probably benign |
|
R9270:Tubb2a
|
UTSW |
13 |
34,258,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Tubb2a
|
UTSW |
13 |
34,260,607 (GRCm39) |
missense |
probably benign |
|
|